3 Jan 2014: Huang KW, Chen HH, Yang HC, Horng HE, Liao SH, et al. (2014) Correction: Discriminating Hepatocellular Carcinoma in Rats Using a High-Tc SQUID Detected Nuclear Resonance Spectrometer in a Magnetic Shielding Box. doi: info:doi/10.1371/annotation/f0b887f3-4636-4f29-ab81-a169247a3ad5 View correction
In this study, we report the spin-lattice relaxation rate of hepatocellular carcinoma (HCC) and normal liver tissue in rats using a high-Tc superconducting quantum interference device (SQUID) based nuclear magnetic resonance (NMR) spectrometer. The resonance spectrometer used for discriminating liver tumors in rats via the difference in longitudinal relaxation time in low magnetic fields was set up in a compact and portable magnetic shielding box. The frequency-domain NMR signals of HCC tissues and normal liver tissues were analyzed to study their respective longitudinal relaxation rate T1−1. The T1−1 of liver tissues for ten normal rats and ten cancerous rats were investigated respectively. The averaged T1−1 value of normal liver tissue was (6.41±0.66) s−1, and the averaged T1−1 value of cancerous tissue was (3.38±0.15) s−1. The ratio of T1−1 for normal liver tissues and cancerous liver tissues of the rats investigated is estimated to be 1.9. Since this significant statistical difference, the T1−1 value can be used to distinguish the HCC tissues from normal liver tissues. This method of examining liver and tumor tissues has the advantages of being convenient, easy to operate, and stable.
Citation: Huang K-W, Chen H-H, Yang H-C, Horng H-E, Liao S-H, Yang SY, et al. (2012) Discriminating Hepatocellular Carcinoma in Rats Using a High-Tc SQUID Detected Nuclear Resonance Spectrometer in a Magnetic Shielding Box. PLoS ONE 7(10): e47057. doi:10.1371/journal.pone.0047057
Editor: Yujin Hoshida, Mount Sinai School of Medicine, United States of America
Received: April 6, 2012; Accepted: September 7, 2012; Published: October 5, 2012
Copyright: © Huang et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This work was supported by the National Science Council of Taiwan under grant number NSC99-2112-M002-017-MY3, NSC 100-2120-M-002-015, NSC101-2120-M168-001, and the Department of Health under grant number DOH100-TD-N-111-008, DOH101-TD-N-111-004. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: One author, Dr. Shieh Yueh Yang, plays two roles of CEO in MagQu Co. and Adjuct Professor in National Taiwan Normal University. He jointed the reseach project (i.e. the declared funding in the manuscript) as his academic role. This does not alter the authors’ adherence to all the PLOS ONE policies on sharing data and materials.
Though sharing the same origin, there are still some morphologic distinctions that exist between normal and cancerous tissue. Nowadays, trained pathologists can discern the differences with certain kinds of immunohistochemical staining under microscopic examination. These are well-accepted tools for confirming the diagnosis of malignant diseases, and are also the main approach we employed to evaluate unknown specimens obtained from biopsy. Recently, a paper on the use of ultrasonography, computed tomography, and magnetic resonance imaging of hepatocellular carcinoma for improved treatment decision was reported . While a different approach, the development of NMR measurement using SQUID detection in low magnetic fields –, has been reported as well. The SQUID-detected magnetic resonance imaging shows promising applications for tumor detection as reported in , and has received much attention recently. Previously, we established a high-Tc SQUID-based low magnetic field nuclear magnetic resonance (NMR) system to measure the longitudinal relaxation rate T1−1 of tap water in a magnetically shielded environment , where T1−1 is the spin-lattice relaxation rate. While recently, we have established a SQUID-based NMR and MRI with radio frequency shielding and a high-Tc SQUID detector in superconducting shielding . Since different tissues should show different T1−1. The T1−1 value is believed to also vary between normal and cancerous tissues. The goal of this research is to develop a novel diagnostic tool that is reliable, stable and more convenient than traditional methods in conducting pathological examinations with a resonance spectrometer set up in a compact and portable magnetic shielding box. Among miscellaneous cancers, hepatocellular carcinoma (HCC) is the most important malignancy in Asia , so we used HCC and normal liver parenchyma of rats as our first experiment subject to appraise the method’s feasibility.
Materials and Methods
10 six-week-old male Wistar rats were chosen for the experiment. All rats were fed water mixed with 100 ppm of diethylnitrosamine for six weeks to induce HCC. All experiments were conducted with the approval of the Institutional Animal Care Committee. After six weeks, the rats’ livers developed tumors of 3–10 mm in diameter . The rats were then euthanized via CO2 inhalation and the livers were harvested. Normal liver parenchyma and tumor tissues were stored separately in liquid nitrogen. Parts of the specimens were stored in formalin solution and hematoxylin, and then eosin staining was performed for prospective pathological studies. The pathologic diagnosis was independently made by two other pathologists to identify liver and tumor tissues.
In the past, the high-Tc SQUID-based NMR/MRI measurements were set up inside a magnetically shielded room . Different from that system, the present resonance spectrometer was set up in a compact and portable magnetic shielding box. So far, it has been used to study the images of chili  and hyperpolarized 3He . In this study, this NMR system was further optimized to discriminate tumors by characterizing the spin-lattice relaxation rate of HCC.
Figure 1 shows a schematic of the compact SQUID-detected resonance spectrometer. The system is consisted of two parts. Part one is consisted of the pre-polarization coil for generating Bp, measuring coil for B0, pulse coil for B1, compensation coil for Bc, and gradient coils for Gz. These coils were setup inside an electromagnetically shielded box of four-layer aluminum. The vertical component of the Earth’s magnetic field, which was perpendicular to the measurement field, was compensated using the compensation coil. The stray gradient field was compensated using a gradient coil. The function of B1-coil is to generate a sinusoidal signal f(t) = A1sin(ωt), where A1 is the amplitude, ω is the resonance frequency which is equal to the Larmor frequency of protons. The pick-up coil inside part one and the input coil inside part two formed a tuned tank circuit, which resonates at the proton’s Larmor frequency with a Q-value of 20. The pick-up coil had an inner diameter of 6 mm, an inductance of ∼2.0 mH and was wound around the samples. The pick-up coil was placed inside the pre-polarization coil. The input coil had an inner diameter of 2.6 cm, coil length of 4 cm, inductance of ∼0.12 mH and was wound around the high-Tc SQUID detector. Part two is consisted of the high-Tc SQUID magnetometer, input coil, Bi2Sr2Ca2Cu3Oy vessel and magnetically shielded cylinder. The magnetically shielded cylinder (MSC) was made of three-layer mu-metal and aluminum plates. A photograph of the MSC is shown in Figure 2(a) and its shielding factor is shown in Figure 2(b). The shielding factor is defined as 20 log(Bshielded/Bunshielded), where Bshieded and Bunshielded are the magnetic field strength inside and outside the magnetically shielded box, respectively. The shielding factor of the MSC is 60 dB at 10 Hz and 55 dB at 1 k Hz. The high-Tc SQUID magnetometer and input coil were placed inside a superconducting vessel that was put in a liquid nitrogen dewar. The dewar was installed inside the mu-metal cylinder. The NMR signal of proton was inductively coupled to the SQUID magnetometer through a tuned tank circuit. Gradient coils were constructed for generating the gradient fields, Gx, Gy, and Gz. After optimizing the NMR signals by using a high pre-polarization field and compensated gradient field, a signal-to-noise ratio of 120 for 10 ml of tap water was obtained and the frequency-domain spectral linewidth was 0.9 Hz in a single measurement as shown in Figure 3. This is comparable to the SQUID-based NMR system in a magnetically shielded environment . The effective transverse relaxation time T2* for the deionized water is T2* = 1 s and the T2 = 2.2 s was derived from the spin-echo measurement at 24°C .
(A) Photograph, and (B) shielding factor.
(A) NMR signal, and (B) frequency-domain NMR spectrum.
The procedures for T1 measurements are shown in Figure 4(a). In NMR measurements, the static field B0 of 100 µT was applied along the z-axis and the pre-polarization field Bp of 70 mT was applied along the x-axis. Since the pre-polarization field’s strength was much stronger than the static measuring field, the direction of the net nuclear spin magnetization of 1H aligned close to the x-axis. After applying a pre-polarization field for the time tBp, the pre-polarization field was turned off in 3 ms. In the presence of the static field B0, the spin magnetization of 1H first processed inside the x-y plane and finally relaxed to the direction of z-axis. The free induction decay NMR signal was then recorded through the band pass filter and amplifier. As an example, the FID NMR signal of 1H nuclear spin for 1.3 gram of normal liver tissues in 10-average was recorded as shown in Figure 4(b). The frequency-domain NMR spectrum is shown in Figure 4(c), which shows a SNR of 3. The peak at 4.41 kHz is the resonance frequency of proton’s spins while the two side peaks are the 60 Hz harmonics.
(A) Procedures applied for measuring the NMR signal of liver tissues, (B) FID of the NMR signal, and (C) frequency-domain NMR spectrum after 10 averages.
To investigate the detection sensitivity of weight, both specimens of normal liver and HCC were divided into 5 pieces by weights that varied from 0.23 to 1.4 gram. The T1−1 value of each sample was measured in a triplet. Next, each liver and tumor sample were divided equally into four different groups with the same weight: Group A was stored at 300 K, Group B was frozen at the liquid nitrogen temperature (77.4 K) for examinations under a frozen status, Group C was also frozen in 77.4 K then defrosted to 300 K before any examinations were performed and frozen again after the experiment, while Group D was preserved in formalin solution. The T1−1 value of specimens in every group was obtained on the 1st, 2nd, 3rd, 4th, 5th, 6th, 7th, 30th, and 60th day of experiments. In the end, each specimen was measured using a commonly used sample holder made from polyvinylchloride, glass, plastic and plastic wrap. The same evaluation was performed to see if the materials of sample holders would affect the T1−1 value or not.
Figure 5 shows the normalized intensity of NMR signals as a function of the pre-polarization time tBp for HCC tissues and normal liver tissues of rat. The data were normalized to the strength of saturated NMR signals to distinguish the signal characteristics for HCC tissues and normal liver tissues. The detected NMR signals Sy(t) as a function of tBP follows the formula:(1)where T1 is the longitudinal relaxation time, T2* is the effective transverse relaxation time and ω is the Larmor frequency of protons in the measuring magnetic field. The peak strength of frequency-domain NMR signal, as a function of tBp, is fitted to [1- exp(−tBp/T1)] to derive the T1 for tissues of HCC and normal livers. The dashed lines in Figure 5 are the fitting curves. 1/T1,normal was equal to (5.96±0.61) s−1 (T1,normal = 167.5 ms) and the 1/T1,tumor was equal to (3.21±0.22) s−1 (T1,tumor = 311.5 ms). The ratio (1/T1,normal)/(1/T1,tumor ) is 1.86.
Figures 6(a) and 6(b) shows the normalized peak strength of the frequency-domain NMR signal as a function of tBp for different weights of the liver tumor and normal liver from the same rat. The solid lines are the fitting curves to [1- exp(−tBp/T1)]. Figure 6(c) shows the derived T1’s for different weights of normal tissues and tumor tissues. The data of T1−1 under different weight conditions helped us come to several conclusions. First we found that the minimum specimen weight that can register a stable T1−1 value is 0.85 grams for normal liver tissue, and 0.23 grams for tumor tissue. Specimens with a weight greater than these values have a statistically stable T1−1 value. Therefore, 0.85 grams of liver tissues and 0.23 grams of tumor tissues are the minimum specimen weights that can be presently measured for the established system. The detection sensitivity of weight for cancerous tissues can be less than 0.23 grams if the system is further optimized by increasing the pre-polarization field’s strength and using a pickup coil in gradient configuration.
(A) Different weight of the tumor in rat’s liver, (B) different weight of rat’s liver, and (C) T1−1 as a function of different weights of rat’s liver tissue and tumor tissue.
Figure 7 shows the averaged T1−1 of liver’s tissues derived from 10 normal rats and 10 HCC rats. The averaged T1−1 value of normal liver tissue is (6.41±0.66) s−1, and the averaged T1−1 value of cancerous tissue is (3.38±0.15) s−1. The averaged T1−1 ratio between normal liver tissues and cancerous tissues is 1.9. The value suggests significant statistical difference between normal liver and cancerous tissues with p<0.05. The feasibility of using T1−1 values to discriminate cancerous liver tissues from normal liver is demonstrated. We note the experimental results of T1-relaxation in Figure 5 and 7 differ depending on the weight, storage time, portion of malignant tissues and environmental noises. The environmental noises can be improved by a pickup coil in gradient configuration and a high-Tc SQUID gradiometer . The present system shows a minimum detection weight of 0.2 g. Increasing the weight of specimens to 0.6 g (see figure 6) can guarantee the accuracy of T1-relaxation measurements. Regarding the storage method, the experimental results show that it is highly recommended to store the samples in liquid nitrogen to preserve the T1-relaxation of tissues.
Samples are derived from ten normal rats and ten HCC rats.
The water contents of normal and tumor tissues were studied in reference . It was found that the data for malignant tissues show a clear trend towards increased water content. The observed difference between relaxation rates is attributed to greater tissue hydration in the neoplasms. In the present study, we demonstrate that (T1−1)normal>(T1−1)tumor using a resonance spectrometer set up in a compact and portable magnetic shielding box.
Since tumor and normal samples are usually preserved in liquid nitrogen or formalin. It was interesting to investigate how many times we could recycle the samples without destroying the T1−1 characteristics. Figure 8 shows ten repeated T1−1 measurements at 300 K for a rat’s liver tissue and tumor tissue when they are thermally cycled from a liquid nitrogen environment. The total time including the warming up time (30 minutes) and the measurement time (15 minutes) in each T1−1 measurement was 45 minutes. The results show that the T1−1 value does not vary significantly and therefore the specimen can be stored at 77.4 K for a long period of time without deteriorating the T1−1. However, if the fresh specimen was not preserved and was kept at 300 K, the T1−1 value would continue to decrease as time proceeded, as shown in Figure 9(a). The T1−1 decreases significantly after exposure to air for two days while the liver tissues degrade. Samples preserved at 77.4 K and recycled to 300 for T1-measurement show no degrading after several days shown in figure 9(b). On the other hand, for the specimen that was preserved in formalin, the most common method of storing specimens, under the aforementioned conditions, we still were able to obtain consistent T1−1 values for sixty testing days.
Samples are rat’s normal liver tissue and tumor tissue when they are thermally cycled from liquid nitrogen.
It is kept at (A) 300 K, and (B) 77.4 K and recycled to 300 K.
The T1−1 of normal liver tissues and HCC tissue was also characterized using different specimen holders consisted of non-magnetic materials such as polyvinylchloride, plastics, plastic wrap, and glass. The results yield no statistical differences in T1−1 values due to the short relaxation rate of sample holders compared with that of the liver tissues. Therefore, we conclude that the T1−1 value is not influenced by nonmagnetic materials that are generally used to hold the specimen.
Currently, the main method of distinguishing normal liver tissues from HCC tissue depends on the pathological analysis of specimen obtained from biopsy. Such examination demands high human resource as this requires professional pathologists and it takes time. Moreover, when the quantity of specimen is undersize, there is usually an insufficient amount to conduct all the examinations. Therefore, the same small piece of specimen may need to be used for regular microscopic examination under the hematoxylin and eosin staining as well as many other immunohistochemical staining simultaneously for coming to a diagnosis. Furthermore, sometimes the specimens are depleted and unable to be used in follow-up pathological examinations. One characteristic of the method described here is that the specimen is not damaged. It can be used for other pathological analysis. This can provide more possibilities when examining undersized specimens.
In the present work, a resonance spectrometer set up in a compact and portable magnetic shielding box was optimized to discriminate tumor tissues from normal liver tissues. The averaged T1−1 value of normal liver tissue is characterized to be (6.41±0.66) s−1, and the averaged T1−1 value of cancerous tissue is (3.38±0.15) s−1. The (T1,normal−1)/(T1,tumor−1) was characterized to be 1.9, which is consistent with the previous results  measured in a magnetically shielded environment. Additionally, the tissues simply need to be stored in liquid nitrogen or preserved in formalin to maintain their efficacy. The present system is compact, the measurement is easy, and the system cost is lower. Therefore, it can also be a promising tool for characterizing different tumors by the parameter T1−1.
In this study, we conclude that in 295 K, a stable T1−1 value can be measured for liver tissues of certain sizes without introducing irrelevant effects from the materials of containers. In addition, the tissues simply need to be stored in liquid nitrogen or preserved in formalin to maintain their efficacy. This method of examining and distinguishing liver and tumor tissues displays the advantages of being convenient, easy to operate, stable, and other benefits. Finally and most importantly, the noticeable difference in the T1−1 value between liver and tumor tissues provides a new direction of study in liver cancer pathology. This warrants further investigation of whether the T1−1 value of tumor tissues can be used to further distinguish various types of tumors.
Conceived and designed the experiments: HCY HEH. Performed the experiments: KWH HHC. Analyzed the data: SHL. Contributed reagents/materials/analysis tools: SYY JJC LMW. Wrote the paper: HCY SHL.
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